Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Organometallic complexes ortho metalation

The chiral center most frequently encountered is the asymmetric carbon atom, a tetrahedral C atom, bonded to four different substituents. Chiral centers of this type are known for many other elements (4). However, chiral centers are also found in other polyhedra, e.g., the metal atoms in octahedral compounds containing three bidendate chelate ligands. Chirality axes, present in the atrop isomers of ortho-substituted biaryls, occur in coordination chemistry in appropriately substituted aryl, pyridyl, and carbene metal complexes. Well known examples of planar chirality in organometallic chemistry are ferrocenes, cymantrenes, and benchrotrenes containing two different substituents in 1,2- or 1,3-positions relative to each other (5-5). [Pg.152]


See other pages where Organometallic complexes ortho metalation is mentioned: [Pg.44]    [Pg.794]    [Pg.793]    [Pg.251]    [Pg.3937]    [Pg.411]    [Pg.196]    [Pg.185]    [Pg.257]    [Pg.273]    [Pg.250]    [Pg.87]    [Pg.124]    [Pg.448]    [Pg.185]    [Pg.257]    [Pg.13]    [Pg.558]    [Pg.185]    [Pg.257]    [Pg.125]    [Pg.464]    [Pg.339]    [Pg.375]    [Pg.190]   
See also in sourсe #XX -- [ Pg.203 ]




SEARCH



Metal organometallic complexes

Organometallics organometallic complexes

Ortho metallation

Ortho-metalated complexes

Ortho-metallations

© 2024 chempedia.info